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Welmate Famotidine 20mg

NDC 73581-109 · YYBA Corp

Generic nameFamotidine 20mg
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

73581-109-01 — 100 TABLET in 1 BOTTLE (73581-109-01)

73581-109-20 — 300 TABLET in 1 BOTTLE (73581-109-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72657-113 — Famotidine, 72657-132 — Famotidine, 72789-331 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, 72865-214 — Famotidine, 72865-215 — Famotidine, 73097-017 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 73581-108 — Famotidine 10mg, 76162-300 — famotidine, 76420-712 — FAMOTIDINE, 76420-713 — FAMOTIDINE, 76420-891 — Ibuprofen and famotidine, 79903-115 — famotidine, 80005-119 — FAMOTIDINE, 80425-0329 — Famotidine, 80425-0384 — Ibuprofen and famotidine, 80425-0422 — Ibuprofen and famotidine, 80425-0483 — Ibuprofen and famotidine, +401 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.